{{Rsnum
|rsid=3783799
|Gene=PRKCH
|Chromosome=14
|position=61452498
|Orientation=minus
|GMAF=0.0629
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PRKCH
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 1.5 | 98.5
| HCB | 2.2 | 31.1 | 66.7
| JPT | 6.7 | 35.6 | 57.8
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 31.1 | 66.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}A common SNP only in Asian populations, this SNP and a close neighbor also in [[PRKCH]] gene, [[rs3783799]], have been associated with higher risk for subcortical silent brain infarction, a common form of [[stroke]].

The odds ratio for carriers of a risk allele is 1.27 (CI: 1.09-1.48, p=0.0026) compared to individuals homozygous for the non-risk allele, based on studies of ~300 Japanese patients. {{PMID|18164711}}

{{PMID Auto
|PMID=20602195
|Title=PRKCH gene polymorphism is associated with the risk of severe gastric atrophy
}}

{{PMID|19703523}} Association of PRKCH gene with lacunar infarction in a local Chinese Han population.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}